JPS6338965B2 - - Google Patents

Info

Publication number: JPS6338965B2
Authority: JP; Japan
Prior art keywords: added; cockroaches; ether; cockroach; present
Prior art date: 1979-12-03
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

JP15665379A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5679602A (en

Inventor

Chikao Nishino

Hisao Takayanagi

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Mitsubishi Chemical Corp

Original Assignee

Mitsubishi Chemical Industries Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1979-12-03

Filing date

1979-12-03

Publication date

1988-08-03

1979-12-03 Application filed by Mitsubishi Chemical Industries Ltd filed Critical Mitsubishi Chemical Industries Ltd

1979-12-03 Priority to JP15665379A priority Critical patent/JPS5679602A/ja

1981-06-30 Publication of JPS5679602A publication Critical patent/JPS5679602A/ja

1988-08-03 Publication of JPS6338965B2 publication Critical patent/JPS6338965B2/ja

Status Granted legal-status Critical Current

Links

241001674044 Blattodea Species 0.000 claims description 13
239000005667 attractant Substances 0.000 claims description 7
230000031902 chemoattractant activity Effects 0.000 claims description 6
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 4
239000004480 active ingredient Substances 0.000 claims description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 22
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
239000000877 Sex Attractant Substances 0.000 description 4
239000012046 mixed solvent Substances 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
238000009395 breeding Methods 0.000 description 3
230000001488 breeding effect Effects 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000000034 method Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000000741 silica gel Substances 0.000 description 3
229910002027 silica gel Inorganic materials 0.000 description 3
WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 2
WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 2
XZFDKWMYCUEKSS-UHFFFAOYSA-N 6,6-Dimethylbicyclo[3.1.1]heptan-2-one Chemical compound C1C2C(C)(C)C1CCC2=O XZFDKWMYCUEKSS-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
238000000862 absorption spectrum Methods 0.000 description 2
XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 2
SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 2
229930006722 beta-pinene Natural products 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
OPHUWKNKFYBPDR-UHFFFAOYSA-N copper lithium Chemical compound [Li].[Cu] OPHUWKNKFYBPDR-UHFFFAOYSA-N 0.000 description 2
229940079593 drug Drugs 0.000 description 2
239000003814 drug Substances 0.000 description 2
LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 2
239000002904 solvent Substances 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
XZFDKWMYCUEKSS-BQBZGAKWSA-N (1s,5r)-6,6-dimethylbicyclo[3.1.1]heptan-4-one Chemical compound C1[C@@]2([H])C(=O)CC[C@]1([H])C2(C)C XZFDKWMYCUEKSS-BQBZGAKWSA-N 0.000 description 1
QKGNSWNKNMFYRE-UHFFFAOYSA-N 2,6,6-trimethylbicyclo[3.1.1]heptan-4-one Chemical compound CC1CC(=O)C2C(C)(C)C1C2 QKGNSWNKNMFYRE-UHFFFAOYSA-N 0.000 description 1
241000238660 Blattidae Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
229910021595 Copper(I) iodide Inorganic materials 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
239000012300 argon atmosphere Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
238000004440 column chromatography Methods 0.000 description 1
LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
238000010828 elution Methods 0.000 description 1
BLHLJVCOVBYQQS-UHFFFAOYSA-N ethyllithium Chemical compound [Li]CC BLHLJVCOVBYQQS-UHFFFAOYSA-N 0.000 description 1
239000011888 foil Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
125000000468 ketone group Chemical group 0.000 description 1
238000001819 mass spectrum Methods 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
230000001766 physiological effect Effects 0.000 description 1
-1 propionyloxy group Chemical group 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

JP15665379A 1979-12-03 1979-12-03 Cockroach attractant Granted JPS5679602A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP15665379A JPS5679602A (en)	1979-12-03	1979-12-03	Cockroach attractant

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP15665379A JPS5679602A (en)	1979-12-03	1979-12-03	Cockroach attractant

Publications (2)

Publication Number	Publication Date
JPS5679602A JPS5679602A (en)	1981-06-30
JPS6338965B2 true JPS6338965B2 (cs)	1988-08-03

Family

ID=15632346

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP15665379A Granted JPS5679602A (en)	1979-12-03	1979-12-03	Cockroach attractant

Country Status (1)

Country	Link
JP (1)	JPS5679602A (cs)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0610122B2 (ja) *	1986-10-14	1994-02-09	大正製薬株式会社	ゴキブリの摂食刺激剤
GB0130577D0 (en) *	2001-12-21	2002-02-06	Univ Keele	Method of monitoring/controlling thysanoptera

1979
- 1979-12-03 JP JP15665379A patent/JPS5679602A/ja active Granted

Also Published As

Publication number	Publication date
JPS5679602A (en)	1981-06-30

Publication	Publication Date	Title
FR2599739A1 (fr)	1987-12-11	Acides biphenyl hydroxamiques a action therapeutique
US5728376A (en)	1998-03-17	Tetradecatrienyl and tetradecadienyl acetates and their use as sex attractants for tomato pests
US4364931A (en)	1982-12-21	Composite insect attractant for male white-line dart moths and a process for preparing the active ingredients thereof
Kuwahara	1980	Isolation and identification of male-secreted possible sex pheromone from a Pyralid moth, Aphomia gularis Zeller (Pyralidae: Lepidoptera)
LaForge et al.	1944	A new constituent isolated from southern prickly-ash bark
JPS623825B2 (cs)	1987-01-27
JP2958169B2 (ja)	1999-10-06	殺ダニ剤
EP3592753B1 (fr)	2022-02-16	Nouvelle composition d'isomeres du 7,9-dodécadiényl-1-acétate et son procede de fabrication
Herz et al.	1981	Structures of the rolandrolides and isorolandrolides, unusual germacradienolides from Rolandra fruticosa
JPS6249241B2 (cs)	1987-10-19
US5505951A (en)	1996-04-09	Cockroach attractant
JP2942408B2 (ja)	1999-08-30	有害生物忌避剤
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AU8050894A (en)	1995-05-08	Novel spin-trap molecule 2-trifluoromethyl-dmpo
Boese Jr et al.	1934	An investigation of certain derivatives of alkyl γ-oxalylcrotonates
JP2569429B2 (ja)	1997-01-08	タイワンキドクガの卵寄生蜂の誘引剤
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JP2569430B2 (ja)	1997-01-08	タイワンキドクガの性誘引剤
JP2007284400A (ja)	2007-11-01	フジコナカイガラムシの性誘引剤
JP2840142B2 (ja)	1998-12-24	２−（１−ヒト゛ロキシ−イソフ゜ロヒ゜ル）−５−メチル−シクロヘ゜ンタノール
RU1396516C (ru)	1993-11-15	Феромон дл листовертки узкокрылой изменчивой CNEPHASIA CHRYSANTHEANA DUP
JPH0616581A (ja)	1994-01-25	新規カウラン型ジテルペン類、その製造法及び該化合物を有効成分とするシロアリ防除剤
Dreiding et al.	1953	The Structure of the Solid Product from the Condensation of Methyl γ-Bromocrotonate with Sodium Methoxide1
JPH0122254B2 (cs)	1989-04-25